Allele Registry

Canonical Allele Identifier: PA658673134

Gene: MSH2 HGNC NCBI

ClinVar Variation Id: 455575

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Gln861Leu	CA346731004 NM_000251.3:c.2582A>T